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刘宁朴老师介绍
姓名：刘宁朴 性别：男 职称：主任医师
职务：眼底专科主任 招生院所：附属同仁医院
招生类型：科学与专业学位(博) 科学与专业学位(硕)
招生专业：眼科学(博) 眼科学(硕)
研究方向名称：玻璃体视网膜疾病
电子信箱：nliu001@gmail.com
社会任职
个人简历
1. 1986-1990:北京医科大学研究生院 博士研究生
2. 1990-1991:Oxford University, UK. Research Fellow
3. 1993-1995:北京医科大学第三医院眼科 副主任医师，副教授
4. 1995-1998:Duke University Eye Center, USA. Postdoctoral Fellow
5. 1998-2000:Duke University Eye Center, USA. Assitant Professor, Member of Faculty
6. 2001-2006:首都医科大学附属北京同仁医院眼科 主任医师
7. 2002-2007:首都医科大学附属北京同仁医院眼科 眼底专科主任
重要学术论文
1. 徐军，樊文英，马凯，杨秀芬，刘宁朴*.玻璃体手术治疗老年性黄斑变性玻璃体积血. 中华眼底病杂志. 2008,24(1):61-62.无
2. 张彦来，徐军，刘宁朴*.玻璃体手术治疗增殖性糖尿病视网膜病变的预后观察. 重庆医科大学学报. 2008,33(2):226-228.无
3. 刘宁朴*，刘熙朴，张惠蓉.关于医学专业学位研究生和住院医师临床能力培养的思考. 中国高等医学教育. 2008,3:104-106.无
4. Xu Y, Guan N, Xu J, Yang X, Ma K, Zhou H, Zhang F, Snellingen T, Jiao Y, Liu X, Wang N, Liu N*.Association of CFH, LOC387715, and HTRA1 polymorphisms with exudative age-related macular degeneration in Northern Chinese. Mol Vis. 2008,14:accepted.SCI
5. 徐玉乐，刘宁朴*.年龄相关性黄斑变性致病危险因素. 国际眼科纵览. 2007,31(3):206-209.无
6. 杨秀芬，刘宁朴*，徐军.年龄相关性黄斑变性的遗传学研究. 国际眼科纵览. 2007,31(3):210-213.无
7. 张宁，韩毳，马凯，徐军，刘守彬，杨庆松，熊颖，刘宁朴*.中心晕轮状黄斑营养障碍家系的临床研究和致病基因分析. 眼科. 2007,16(4):241-245.无
8. 韩毳，张宁，刘熙朴，刘宁朴*.原因不明的黄斑区视网膜前出血二例. 眼科. 2007,16(4):285-287.无
9. Wang J, Ma X, Gu F, Liu NP, Hao XL, Wang KJ, Wang NL, Zhu SQ*.A Missense Mutation S228P in the CRYBB1 Gene Causes Autosomal Dominant Congenital Cataract. Chin Med J . 2007,120(9):820-824.SCI
10. 张宁,段欣荣,韩毳,陈惠茹,张风,刘宁朴*.视网膜脱离复位手术后交感性眼炎二例. 眼科. 2006,15（4）:285-286.无
11. Liu NP, Smith CF, Bowling BL, Jonasson F, Klintworth GK. .Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland. Mol Vis . 2006,12:1148-1152.SCI
12. 朱思泉，刘宁朴*，王宁利，陈辉.双手微切口白内障超声乳化手术的初步临床应用. 眼科 . 2006,15:24-27.无
13. 卢海，刘宁朴，卢宁，刘武.糖尿病视网膜病变玻璃体切除术中晶状体的处理. 眼科. 2005,14（4）:275-277.无
14. Liu NP, Bao W, Smith CF, Vance JM, Klintworth GK.Different mutations in carbohydrate sulfotransferase 6 (CHST6) gene cause macular corneal dystrophy types I and II in a single sibship.. Am J Ophthalmol. 2005,139（6）:1118-1120.SCI
15. 4. Allingham RR, Seo B, Rampersaud E, Bembe M, Challa P, Liu N, Parrish T, Karolak L, Gilbert J, Pericak-Vance MA, Klintworth GK, Vance JM.A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis. Am J Hum Genet. 2001,68:491-494.SCI
16. Liu NP, Dew-Knight S, Rayner M, Jonasson F, Akama TO, Fukuda MN, Bao W, Gilbert JR, Vance JM, Klintworth GK.Mutations in carbohydrate sulfotransferase 6 (CHST6) gene cause macular corneal dystrophy type I in Iceland. . Mol Vis. 2000,6:261-264.SCI
17. Liu NP, Dew-Knight S, Jonasson F, Gilbert JR, Klintworth GK, Vance JM.Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes.. Mol Vis . 2000,6:95-100.SCI
18. Liu NP, Baldwin J, Lennon F, Stajich JM, Thonar EJ-MA, Pericak-Vance MA, Klintworth GK, Vance JM.Coexistence of macular corneal dystrophy types I and II in a single sibship.. Br J Ophthalmol . 1998,82:241-244.SCI
19. Liu NP, Baldwin J, Jonasson F, Dew-Knight S, Stajich JM, Lennon F, Pericak-Vance MA, Klintworth GK, Vance JM.Haplotype analysis in Icelandic families defines a minimal interval for macular corneal dystrophy type I gene. . Am J Hum Genet. 1998,63:912-917.SCI
20. Liu NP, Roberts WL, Hale LP, Levesque MC, Patel DD, Lu CL, Jaffe GJ.Expression of CD44 and variant isoforms in cultured human retinal pigment epithelium cells.. Invest Ophthalmol Vis Sci. 1997,38:2027-2037.SCI
21. 10. Osborne NN, FitzGibbon F, Nash M, Liu NP, Leslie R, Cholewinski A.Serotonergic, 5-HT2, receptor-mediated phosphoinositide turnover and mobilization of calcium in cultured rat retinal pigment epithelial cells. Vision Res. 1993,33:2171-2179.SCI
22. Liu NP, FitzGibbon F, Nash M, Osborne NN.Epidermal growth factor potentiates the transmitter-induced stimulation of C-AMP and inositol phosphates in human retinal pigment epithelium cells in culture.. Exp Eye Res. 1992,55:489-497.SCI
主编或副主编的著作/译著
1. 《眼底病图谱》,副主编,人民卫生出版社,200706
重要奖项
1. 培养视网膜色素上皮细胞膜受体和受体间交互作用研究 北京医科大学科技进步奖 199509
职务：眼底专科主任 招生院所：附属同仁医院
招生类型：科学与专业学位(博) 科学与专业学位(硕)
招生专业：眼科学(博) 眼科学(硕)
研究方向名称：玻璃体视网膜疾病
电子信箱：nliu001@gmail.com
社会任职
个人简历
1. 1986-1990:北京医科大学研究生院 博士研究生
2. 1990-1991:Oxford University, UK. Research Fellow
3. 1993-1995:北京医科大学第三医院眼科 副主任医师，副教授
4. 1995-1998:Duke University Eye Center, USA. Postdoctoral Fellow
5. 1998-2000:Duke University Eye Center, USA. Assitant Professor, Member of Faculty
6. 2001-2006:首都医科大学附属北京同仁医院眼科 主任医师
7. 2002-2007:首都医科大学附属北京同仁医院眼科 眼底专科主任
重要学术论文
1. 徐军，樊文英，马凯，杨秀芬，刘宁朴*.玻璃体手术治疗老年性黄斑变性玻璃体积血. 中华眼底病杂志. 2008,24(1):61-62.无
2. 张彦来，徐军，刘宁朴*.玻璃体手术治疗增殖性糖尿病视网膜病变的预后观察. 重庆医科大学学报. 2008,33(2):226-228.无
3. 刘宁朴*，刘熙朴，张惠蓉.关于医学专业学位研究生和住院医师临床能力培养的思考. 中国高等医学教育. 2008,3:104-106.无
4. Xu Y, Guan N, Xu J, Yang X, Ma K, Zhou H, Zhang F, Snellingen T, Jiao Y, Liu X, Wang N, Liu N*.Association of CFH, LOC387715, and HTRA1 polymorphisms with exudative age-related macular degeneration in Northern Chinese. Mol Vis. 2008,14:accepted.SCI
5. 徐玉乐，刘宁朴*.年龄相关性黄斑变性致病危险因素. 国际眼科纵览. 2007,31(3):206-209.无
6. 杨秀芬，刘宁朴*，徐军.年龄相关性黄斑变性的遗传学研究. 国际眼科纵览. 2007,31(3):210-213.无
7. 张宁，韩毳，马凯，徐军，刘守彬，杨庆松，熊颖，刘宁朴*.中心晕轮状黄斑营养障碍家系的临床研究和致病基因分析. 眼科. 2007,16(4):241-245.无
8. 韩毳，张宁，刘熙朴，刘宁朴*.原因不明的黄斑区视网膜前出血二例. 眼科. 2007,16(4):285-287.无
9. Wang J, Ma X, Gu F, Liu NP, Hao XL, Wang KJ, Wang NL, Zhu SQ*.A Missense Mutation S228P in the CRYBB1 Gene Causes Autosomal Dominant Congenital Cataract. Chin Med J . 2007,120(9):820-824.SCI
10. 张宁,段欣荣,韩毳,陈惠茹,张风,刘宁朴*.视网膜脱离复位手术后交感性眼炎二例. 眼科. 2006,15（4）:285-286.无
11. Liu NP, Smith CF, Bowling BL, Jonasson F, Klintworth GK. .Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland. Mol Vis . 2006,12:1148-1152.SCI
12. 朱思泉，刘宁朴*，王宁利，陈辉.双手微切口白内障超声乳化手术的初步临床应用. 眼科 . 2006,15:24-27.无
13. 卢海，刘宁朴，卢宁，刘武.糖尿病视网膜病变玻璃体切除术中晶状体的处理. 眼科. 2005,14（4）:275-277.无
14. Liu NP, Bao W, Smith CF, Vance JM, Klintworth GK.Different mutations in carbohydrate sulfotransferase 6 (CHST6) gene cause macular corneal dystrophy types I and II in a single sibship.. Am J Ophthalmol. 2005,139（6）:1118-1120.SCI
15. 4. Allingham RR, Seo B, Rampersaud E, Bembe M, Challa P, Liu N, Parrish T, Karolak L, Gilbert J, Pericak-Vance MA, Klintworth GK, Vance JM.A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis. Am J Hum Genet. 2001,68:491-494.SCI
16. Liu NP, Dew-Knight S, Rayner M, Jonasson F, Akama TO, Fukuda MN, Bao W, Gilbert JR, Vance JM, Klintworth GK.Mutations in carbohydrate sulfotransferase 6 (CHST6) gene cause macular corneal dystrophy type I in Iceland. . Mol Vis. 2000,6:261-264.SCI
17. Liu NP, Dew-Knight S, Jonasson F, Gilbert JR, Klintworth GK, Vance JM.Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes.. Mol Vis . 2000,6:95-100.SCI
18. Liu NP, Baldwin J, Lennon F, Stajich JM, Thonar EJ-MA, Pericak-Vance MA, Klintworth GK, Vance JM.Coexistence of macular corneal dystrophy types I and II in a single sibship.. Br J Ophthalmol . 1998,82:241-244.SCI
19. Liu NP, Baldwin J, Jonasson F, Dew-Knight S, Stajich JM, Lennon F, Pericak-Vance MA, Klintworth GK, Vance JM.Haplotype analysis in Icelandic families defines a minimal interval for macular corneal dystrophy type I gene. . Am J Hum Genet. 1998,63:912-917.SCI
20. Liu NP, Roberts WL, Hale LP, Levesque MC, Patel DD, Lu CL, Jaffe GJ.Expression of CD44 and variant isoforms in cultured human retinal pigment epithelium cells.. Invest Ophthalmol Vis Sci. 1997,38:2027-2037.SCI
21. 10. Osborne NN, FitzGibbon F, Nash M, Liu NP, Leslie R, Cholewinski A.Serotonergic, 5-HT2, receptor-mediated phosphoinositide turnover and mobilization of calcium in cultured rat retinal pigment epithelial cells. Vision Res. 1993,33:2171-2179.SCI
22. Liu NP, FitzGibbon F, Nash M, Osborne NN.Epidermal growth factor potentiates the transmitter-induced stimulation of C-AMP and inositol phosphates in human retinal pigment epithelium cells in culture.. Exp Eye Res. 1992,55:489-497.SCI
主编或副主编的著作/译著
1. 《眼底病图谱》,副主编,人民卫生出版社,200706
重要奖项
1. 培养视网膜色素上皮细胞膜受体和受体间交互作用研究 北京医科大学科技进步奖 199509
